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迈向蛋白质组学中无与伦比的色谱分离能力:综合空间三维液相分离技术的设计与开发

Toward Unrivaled Chromatographic Resolving Power in Proteomics: Design and Development of Comprehensive Spatial Three-Dimensional Liquid-Phase Separation Technology.

作者信息

Eeltink Sebastiaan, De Vos Jelle, Desmet Gert

机构信息

1Department of Chemical Engineering, Vrije Universiteit Brussel, Brussels, Belgium; email:

2Current affiliation: RIC Group, Kortrijk, Belgium.

出版信息

Annu Rev Anal Chem (Palo Alto Calif). 2024 Jul;17(1):475-493. doi: 10.1146/annurev-anchem-061522-044510. Epub 2024 Jul 2.

Abstract

Spatial comprehensive three-dimensional chromatography (3D-LC) offers an innovative approach to achieve unprecedented resolving power in terms of peak capacity and sample throughput. This advanced technique separates components within a 3D separation space, where orthogonal retention mechanisms are incorporated. The parallel development of the second- and third-dimension stages effectively overcomes the inherent limitation of conventional multidimensional approaches, where sampled fractions are analyzed sequentially. This review focuses on the design aspects of the microchip for spatial 3D-LC and the selection of orthogonal separation modes to enable the analysis of intact proteins. The design considerations for the flow distributor and channel layout are discussed, along with various approaches to confine the flow during the subsequent development stages. Additionally, the integration of stationary phases into the microchip is addressed, and interfacing to mass spectrometry detection is discussed. According to Pareto optimality, the integration of isoelectric focusing, size-exclusion chromatography, and reversed-phase chromatography in a spatial 3D-LC approach is predicted to achieve an exceptional peak capacity of over 30,000 within a 1-h analysis, setting a new benchmark in chromatographic performance.

摘要

空间综合三维色谱法(3D-LC)提供了一种创新方法,可在峰容量和样品通量方面实现前所未有的分离能力。这种先进技术在包含正交保留机制的三维分离空间内分离组分。第二维和第三维阶段的并行发展有效地克服了传统多维方法的固有局限性,传统方法中采样馏分是顺序分析的。本综述重点关注用于空间3D-LC的微芯片设计方面以及正交分离模式的选择,以实现完整蛋白质的分析。讨论了流动分配器和通道布局的设计考虑因素,以及在后续开发阶段限制流动的各种方法。此外,还讨论了固定相在微芯片中的集成以及与质谱检测的接口。根据帕累托最优原则,预计在空间3D-LC方法中整合等电聚焦、尺寸排阻色谱和反相色谱,可在1小时分析内实现超过30000的卓越峰容量,为色谱性能设定新的基准。

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